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Results 1 - 10 of 12 for Hearing "loss," autosomal dominant 76
  1. TECTA gene 
    ... mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss. Hum Mutat. 2011 Jul;32(7):825-34. ... zona pellucida domain of alpha-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family. J Med Genet. 2001 ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  2. GJB2 gene 
    ... needed for hearing.DFNA3 is inherited in an autosomal dominant pattern, which means only one mutated copy of the GJB2 gene in each cell is sufficient to cause the condition. This form of hearing loss can be either prelingual or begin after a ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  3. Jackson-Weiss syndrome 
    ... feet. FGFR2 ... Agochukwu NB, Solomon BD, Muenke M. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics
  4. Pfeiffer syndrome 
    ... FGFR1 FGFR2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics
  5. Spondyloepiphyseal dysplasia with metatarsal shortening 
    ... properly. COL2A1 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/...seal-dysplasia-with-metatarsal-shortening - Genetics
  6. 10q26 deletion syndrome 
    ... chromosome 10 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/10q26-deletion-syndrome - Genetics
  7. RRM2B gene 
    ... A. A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions. Am ...
    https://medlineplus.gov/genetics/gene/rrm2b - Genetics
  8. Saethre-Chotzen syndrome 
    ... chromosome 7 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics
  9. Campomelic dysplasia 
    ... dysplasia. SOX9 Campomelic dysplasia is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/campomelic-dysplasia - Genetics
  10. Cerebral cavernous malformation 
    ... unknown. CCM2 KRIT1 PDCD10 This condition has an autosomal dominant pattern of inheritance, which means one copy of ...
    https://medlineplus.gov/.../cerebral-cavernous-malformation - Genetics
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